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J Zeman

Showing results (241-250 of 311) with videos related to

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Mitochondrion|January 26, 2010
Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal developmentM Pejznochova, M Tesarova, H Hansikova, et al.
Ceskoslovenska Pediatrie|July 1, 1986
[Lead poisoning in an infant]J Zeman, P Martásek, A Rubín, et al.
Prague Medical Report|June 14, 2012
Novel mutations in the tyrosine hydroxylase gene in the first Czech patient with tyrosine hydroxylase deficiencyK Szentiványi, H Hansíková, J Krijt, et al.
Journal of the American Chemical Society|April 9, 2020
Excited-State Turn-On of Aurophilicity and Tunability of Relativistic Effects in a Series of Digold Triazolates Synthesized via iClickCharles J Zeman, Yu-Hsuan Shen, Jessica K Heller, et al.
Casopis Lekaru Ceskych|November 18, 1998
[Lactate acidosis in childhood]J Zeman, L Stratilová, H Houst'ková, et al.
Clinical Pediatrics|November 7, 2003
The clinical spectrum of mitochondrial disease in 75 pediatric patientsD Skladal, C Sudmeier, V Konstantopoulou, et al.
Casopis Lekaru Ceskych|April 4, 2000
[Lysosomal acid lipase deficiency. Overview of Czech patients]M Elleder, H Poupĕtová, J Ledvinová, et al.
Folia Biologica|December 12, 2007
A new mutation within the porphobilinogen deaminase gene leading to a truncated protein as a cause of acute intermittent porphyria in an extended Indian familyE Flachsová, I C Verma, D Ulbrichová, et al.
Physiological Research|November 16, 2017
Changes in transcription pattern lead to a marked decrease in COX, CS and SQR activity after the developmental point of the 22(nd) gestational weekH Kolarova, J Krizova, M Hulkova, et al.
Annals of Hematology|August 1, 1994
Hb Nottingham or alpha 2 beta 2 98 (FG5) Val-->Gly in a Czech childV Brabec, K Indrák, H Fortová, et al.
Pageof 32

Showing results (241-250 of 311) with videos related to

Sort By:
Pageof 32
Mitochondrion|January 26, 2010
Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal developmentM Pejznochova, M Tesarova, H Hansikova, et al.
Ceskoslovenska Pediatrie|July 1, 1986
[Lead poisoning in an infant]J Zeman, P Martásek, A Rubín, et al.
Prague Medical Report|June 14, 2012
Novel mutations in the tyrosine hydroxylase gene in the first Czech patient with tyrosine hydroxylase deficiencyK Szentiványi, H Hansíková, J Krijt, et al.
Journal of the American Chemical Society|April 9, 2020
Excited-State Turn-On of Aurophilicity and Tunability of Relativistic Effects in a Series of Digold Triazolates Synthesized via iClickCharles J Zeman, Yu-Hsuan Shen, Jessica K Heller, et al.
Casopis Lekaru Ceskych|November 18, 1998
[Lactate acidosis in childhood]J Zeman, L Stratilová, H Houst'ková, et al.
Clinical Pediatrics|November 7, 2003
The clinical spectrum of mitochondrial disease in 75 pediatric patientsD Skladal, C Sudmeier, V Konstantopoulou, et al.
Casopis Lekaru Ceskych|April 4, 2000
[Lysosomal acid lipase deficiency. Overview of Czech patients]M Elleder, H Poupĕtová, J Ledvinová, et al.
Folia Biologica|December 12, 2007
A new mutation within the porphobilinogen deaminase gene leading to a truncated protein as a cause of acute intermittent porphyria in an extended Indian familyE Flachsová, I C Verma, D Ulbrichová, et al.
Physiological Research|November 16, 2017
Changes in transcription pattern lead to a marked decrease in COX, CS and SQR activity after the developmental point of the 22(nd) gestational weekH Kolarova, J Krizova, M Hulkova, et al.
Annals of Hematology|August 1, 1994
Hb Nottingham or alpha 2 beta 2 98 (FG5) Val-->Gly in a Czech childV Brabec, K Indrák, H Fortová, et al.
Pageof 32